| manager |
|
| language |
- |
| license |
- |
| created at |
2025-11-26 04:53:50 UTC |
| updated at |
2025-11-27 01:00:35 UTC |
|
Mondo ID - Mondo Label
|
30,114 entries
|
There is 0 pattern entry.
|
lipodystrophy due to peptidic growth factors deficiency
|
0009312 |
|
|
non-spherocytic hemolytic anemia due to hexokinase deficiency
|
0009340 |
|
|
3-hydroxyisobutyric aciduria
|
0009371 |
|
|
seizures-intellectual disability due to hydroxylysinuria syndrome
|
0009373 |
|
|
hypoinsulinemic hypoglycemia and body hemihypertrophy
|
0009416 |
|
|
channelopathy-associated congenital insensitivity to pain, autosomal recessive
|
0009459 |
|
|
hereditary palmoplantar keratoderma, Gamborg-Nielsen type
|
0009489 |
|
|
metabolic myopathy due to lactate transporter defect
|
0009501 |
|
|
laryngo-onycho-cutaneous syndrome
|
0009513 |
|
|
3-hydroxy-3-methylglutaric aciduria
|
0009520 |
|
|
Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
|
0009522 |
|
|
lipoid proteinosis
|
0009530 |
|
|
neurocutaneous melanocytosis
|
0009578 |
|
|
porphyria cutanea tarda
|
0015104 |
|
|
chronic mucocutaneous candidiasis
|
0015279 |
|